Vaso-occlusive device having pivotable coupling

ABSTRACT

An assembly for occluding a vascular site (e.g., an aneurysm) of a human or veterinary patient includes a vaso-occlusive member, a pusher member having a distal end and a severable junction located proximal to the distal end, and a pivotable coupling that couples the pusher member to the occlusive member. A delivery catheter can be used to deliver the vaso-occlusive member to the vascular site. A method of using the assembly to occlude an aneurysm having an aneurysmal sac and an aneurysmal neck, includes locating the catheter within the aneurysmal neck, and manipulating the pusher member to place the vaso-occlusive member within the aneurysmal sac. The method further includes severing the severable junction to detach the vaso-occlusive member from the pusher member. As a result, an axial force is applied by the vaso-occlusive member in a proximal direction, which buckles the pivotable coupling to laterally deflect the axial force. The lateral deflection of the axial force caused by the buckling of the pivotable coupling prevents the catheter from being displaced from the aneurysmal neck by the axial force.

RELATED APPLICATION DATA

The present application claims the benefit under 35 U.S.C. §120 to U.S.patent application Ser. No. 11/022,189, filed Dec. 22, 2004. Theforegoing application is hereby incorporated by reference into thepresent application in its entirety.

FIELD OF THE INVENTION

The present invention relates to assemblies for implantingvaso-occlusive devices in-vivo for establishing an embolus or vascularocclusion in a vessel of a human or veterinary patient.

BACKGROUND OF THE INVENTION

Vaso-occlusive devices or implants are used for a wide variety ofreasons. They are often used for treatment of intra-vascular aneurysms.This is to say that the treatment involves the placement of avaso-occlusive device in an aneurysm to cause the formation of a clotand eventually of a collagenous mass containing the vaso-occlusivedevice. These occlusions seal and fill the aneurysm thereby preventingthe weakened wall of the aneurysm from being exposed to the pulsingblood pressure of the open vascular lumen. Treatment of aneurysms inthis fashion is a significant improvement over the surgical methodtypically involved.

A common vaso-occlusive device is a soft, helically wound coil. Atypical commercial coil will be formed by winding a platinum wire strandabout a primary mandrel and applying a heat treatment to impart aprimary winding coil shape. The relative stiffness of the coil willdepend, among other things, on the diameter of the wire strand, thediameter of the primary mandrel, and the pitch of the primary windings.The device is then wrapped around a secondary mandrel, and again heattreated to impart a secondary shape. For example, U.S. Pat. No.4,994,069, to Ritchart et al., describes a vaso-occlusive coil thatassumes a primary, linear helical configuration when stretched and afolded, and a convoluted, secondary configuration when relaxed in aminimal energy configuration. The stretched condition is used in placingthe coil at the desired site (by its passage through a deliverycatheter) and the coil assumes a relaxed configuration—which is bettersuited to occlude the vessel—once the device is so placed.

It is well-known to detach such vaso-occlusive coil devices from adelivery wire using a mechanical detachment mechanism. For example, U.S.Pat. No. 5,234,437, to Sepetka, shows a method of unscrewing a helicallywound coil from a pusher having interlocking surfaces. U.S. Pat. No.5,250,071, to Palermo, shows an embolic coil assembly using interlockingclasps mounted both on the pusher and on the embolic coil. U.S. Pat. No.5,261,916, to Engelson, shows a detachable pusher-vaso-occlusive coilassembly having an interlocking ball and keyway-type coupling. U.S. Pat.No. 5,304,195, to Twyford et al., shows a pusher-vaso-occlusive coilassembly having an affixed, proximally extending wire carrying a ball onits proximal end and a pusher having a similar end. The two ends areinterlocked and disengage when expelled from the distal tip of thecatheter.

It is also well-known to use an electrolytically severable joint torelease vaso-occlusive coils at the vessel site. For example, Guglielmiet al. shows an embolism forming device and procedure for using thatdevice which employs an electrolytically severable joint. Specifically,Guglielmi et al. desirably places a finely wound platinum coil into avascular cavity such as an aneurysm. The coil is deliveredendovascularly using a catheter such as those described above. Afterplacement in the aneurysm, the coil is severed from its insertion corewire by the application of a small electric current to that core wire.The deliverable coils are said to be made of a platinum material.Proximal of the embolic coil, as noted above, is a core wire which istypically stainless steel. The core wire is used to push the platinumembolic coil into vascular site to be occluded. Other variations of theGuglielmi et al. technology are found in U.S. Pat. No. 5,354,295.

Current electrolytically detachable coil products employ a relativelyinflexible bridge assembly that connects the proximal end of thevaso-occlusive coil to the distal end of the pusher wire assembly. Whenthe coil is detached from the pusher wire, the force the pusher wire hasbeen exerting on the coil (and aneurysm wall) pushes back on the pusherwire assembly, which can displace the tip of the introducer catheter outof the aneurysm. This is because the PET sleeve does not laterallybuckle or flex, but instead axially transmits the push-back forceagainst the distal tip of the delivery catheter. Having the catheter tipdisplaced from the aneurysm requires the physician to relocate thecatheter tip prior to placement of a further occlusive device, whichundesirably extends the duration of the procedure.

SUMMARY OF THE INVENTION

In accordance with one aspect of the invention, an assembly is providedfor establishing an embolus or vascular occlusion in a vessel of a humanor veterinary patient. The assembly generally includes a vaso-occlusivemember (e.g., a coil), a pusher member having a distal end and aseverable junction (e.g., a mechanically or electrolytically severablejunction) located proximal to the distal end, and a pivotable couplingthat couples the pusher member to the occlusive device. The assembly mayoptionally comprise a catheter in which the pusher member is slidablydisposed. If the vaso-occlusive member comprises a coil, the assemblymay optionally comprise a stretch-resisting member, in which case, thepivotable coupling may anchor the stretch-resisting member within thelumen of the coil. Besides optionally providing anchoring for astretch-resisting member, the pivotable coupling may also include anelement that electrically insulates the pusher member distal end fromvaso-occlusive member. The pivotable coupling may be fashioned in anyone of a variety of manners.

In one embodiment, the pivotable coupling comprises a flexible sleeve(e.g., one made of an elastomeric material) coupled between the pushermember distal end and vaso-occlusive member. The pivotable coupling mayalso comprise a proximal coil coupled to the pusher member distal end,and a distal coil coupled to the vaso-occlusive member, in which case,the sleeve is disposed over the proximal and distal coils.

In another embodiment, the pivotable coupling comprises a proximal linkmember (e.g., a hook or loop) coupled to the pusher member distal end,and a distal link member (e.g., a hook or loop) coupled to thevaso-occlusive member, wherein the proximal and distal link memberspivotably engage each other. The pivotable coupling may also comprise aproximal coil coupled to the pusher member distal end, and a distal coilcoupled to the vaso-occlusive member, in which case, the proximal linkmember is disposed on a distal end of the proximal coil, and the distallink member is disposed on a proximal end of the distal coil.

In still another embodiment, the pivotable coupling comprises a firstball member coupled to the pusher member distal end, a second ballmember coupled to the vaso-occlusive member, and a sleeve (e.g., a braidor mesh) holding the first and second ball members. The pivotablecoupling may also comprise a coil mounted to the vaso-occlusive member,in which case, the first ball member is formed onto the pusher memberdistal end, and the second ball member is formed on a proximal end ofthe coil.

In yet another embodiment, the pivotable coupling comprises a first coilcoupled between the pusher member distal end and the vaso-occlusivemember. The first coil comprises open-pitched windings between whichspaces reside. The vaso-occlusive member comprises a vaso-occlusive coilcomprising proximal windings disposed within the spaces between some ofthe open-pitched windings. At least some of the spaces between theopen-pitched windings remain empty. The pivotable coupling may comprisesa second coil coupled between the pusher member distal end and the firstcoil, in which case, the second coil comprises distal windings disposedwithin the spaces between some of the open-pitched windings.

In accordance with another aspect of the invention, a method ofoccluding a vascular site (e.g., an aneurysm) using the vaso-occlusiveassembly is provided. The method comprises manipulating the pushermember to place the vaso-occlusive member adjacent the vascular site. Ifthe vascular site is an aneurysm, the delivery catheter can be placedwithin the aneurysmal neck, and the pusher member can be manipulated toplace the vaso-occlusive member within the aneurysmal sac. The methodfurther comprises severing the severable junction to detach thevaso-occlusive member from the pusher member. As a result, an axialforce is applied by the vaso-occlusive member in a proximal direction,which buckles the pivotable coupling to laterally deflect the axialforce. If the catheter is in an aneurysmal neck, the lateral deflectionof the axial force caused by the buckling of the pivotable coupling willprevent the catheter from being displaced from the aneurysmal neck bythe axial force.

Other features of the present invention will become apparent fromconsideration of the following description taken in conjunction with theaccompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

The drawings illustrate the design and utility of preferred embodimentsof the present invention, in which similar elements are referred to bycommon reference numerals. In order to better appreciate how theabove-recited and other advantages and objects of the present inventionsare obtained, a more particular description of the present inventionsbriefly described above will be rendered by reference to specificembodiments thereof, which are illustrated in the accompanying drawings.Understanding that these drawings depict only typical embodiments of theinvention and are not therefore to be considered limiting of its scope,the invention will be described and explained with additionalspecificity and detail through the use of the accompanying drawings inwhich:

FIG. 1 is a cross-sectional view of a vaso-occlusive assemblyconstructed in accordance with a preferred embodiment of the presentinventions;

FIG. 2 is a cross-sectional view of the vaso-occlusive assembly of FIG.1, particularly illustrating operation of a pivotable coupling withinthe assembly;

FIG. 3 is a cross-sectional view of a vaso-occlusive assemblyconstructed in accordance with another preferred embodiment of thepresent inventions;

FIG. 4 is a cross-sectional view of the vaso-occlusive assembly of FIG.3, particularly illustrating operation of a pivotable coupling withinthe assembly;

FIG. 5 is a cross-sectional view of a vaso-occlusive assemblyconstructed in accordance with still another preferred embodiment of thepresent inventions;

FIG. 6 is a cross-sectional view of the vaso-occlusive assembly of FIG.5, particularly illustrating operation of a pivotable coupling withinthe assembly;

FIG. 7 is an exploded view of a pivotable coupling and vaso-occlusivecoil used in the vaso-occlusive assembly of FIG. 5;

FIG. 8 is a cross-sectional view of a vaso-occlusive assemblyconstructed in accordance with yet another preferred embodiment of thepresent inventions;

FIG. 9 is a cross-sectional view of the vaso-occlusive assembly of FIG.8, particularly illustrating operation of a pivotable coupling withinthe assembly;

FIG. 10 is an exploded view of a pivotable coupling and vaso-occlusivecoil used in the vaso-occlusive assembly of FIG. 8, and

FIGS. 11A-11C illustrate a method of using the vaso-occlusive assemblyof FIG. 1 to occlude an aneurysm.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Referring to FIG. 1, a vaso-occlusive assembly 10 constructed inaccordance with a preferred embodiment is illustrated. For purposes oforientation, the term “proximal” as it qualifies an element generallyrefers to the left end of the element, and the term “right” as it refersto an element generally refers to the right end of the element, as shownin the figures. The vaso-occlusive assembly 10 generally comprises adelivery device 12, which includes an elongated tubular catheter 16 anda pusher member 18, and a vaso-occlusive device 14 detachably associatedwith the distal end of the delivery device 12, and in particular, thedistal end of the pusher member 18.

The catheter 16 comprises an elongated tubular member 20 having adelivery lumen 22 in which the pusher member 18, and thus, thevaso-occlusive device 14, is slidably disposed. The tubular member 20can be composed of any suitable flexible and biocompatible material thatallows it to be introduced through the tortuous vasculature of a patientto the vascular occlusion site. The pusher member 18 has a severablejunction 24 that operates to selectively detach the vaso-occlusivedevice 14 from the delivery device 12. In the illustrated embodiment,the severable junction 24 is an electrolytically severable junction thatis susceptible to electrolysis, and thus, disintegrates when the corewire 18 is electrically charged in the presence of an ionic solution,such as blood or most other bodily fluids.

To provide the electrical charge, the catheter 16 further comprises anannular electrode 26 mounted on the tubular member 20 at the distal endof the delivery lumen 22 and electrical conductors 28 (two shown)axially extending through the wall of the tubular member 20 in contactwith the electrode 26. The electrode 26 comprises a conductivebiocompatible material, such as stainless steel, titanium, copper,platinum, gold, silver, or alloys thereof. Thus, when theelectrolytically severable junction 24 is disposed outside of thecatheter 16 in contact with the bodily fluids of the patient, electricalenergy can be transmitted through the conductors 28 to the electrode 26,where it is transmitted to the portion of the core wire 18 in contactwith the electrode 26. The electrical energy is then transmitted throughthe core wire 18 to the electrolytically severable junction 24, whichundergoes electrolysis until it severs to detach the vaso-occlusivedevice 14 from the delivery device 12. Further details regarding the useof electrolytic joints are described in U.S. Pat. Nos. 5,354,295,5,122,136, and 5,941,888, which are expressly incorporated herein byreference.

It should be noted that other types of severable junctions, such asmechanically severable junctions, can also be used to connect thevaso-occlusive device 14 to the pusher member 18. Various mechanicalmechanisms are described in U.S. Pat. Nos. 5,234,437, 5,250,071,5,261,916, 5,304,195, 5,312,415, and 5,350,397, which are expresslyincorporated herein by reference.

Referring still to FIG. 1, the vaso-occlusive device 14 includes avaso-occlusive member 30 having a lumen 32 extending therethrough, astretch-resisting member 34 extending within the lumen 32 of thevaso-occlusive member 30 to prevent axial stretching of thevaso-occlusive member 30, and a pivotable coupling 36 that operates toaffix the vaso-occlusive member 30 to the core wire 18, while providinga pivot point 38 about which the distal end of the pusher member 18 andthe vaso-occlusive member 30 pivot in order to deflect an axial forceotherwise applied to the delivery device 12 by the vaso-occlusive device14 after the junction 24 has been severed. In the illustratedembodiment, the pivotable coupling 36 also serves as an anchoringassembly that facilitates anchoring of the stretch-resisting member 34within the vaso-occlusive member 30.

The vaso-occlusive member 30 has a sufficient small size that enables itto be advanced through the delivery catheter 16 and access the targetedvascular site. The materials used in constructing the vaso-occlusivemember 30 may be any of a wide variety of materials, and preferably, aradio-opaque and biologically compatible material. Suitable metallicmaterials include the Platinum Group metals, especially platinum,rhodium, palladium, rhenium, as well as tungsten, gold, silver,tantalum, and alloys of these metals. Highly preferred is aplatinum/tungsten alloy, e.g., 8% tungsten and the remainder platinum.Certain polymers can also be used as a suitable material for thevaso-occlusive member 30 either alone or in conjunction withradio-opaque markers, e.g., by filling the polymer with radio-opaquematerial, such as powdered tantalum, powdered tungsten, bismuth oxide,barium sulfate, and the like.

In the illustrated embodiment, the primary vaso-occlusive member 30takes the form of a helical coil with windings 40, although othersuitable members, such as a ribbon, a braided member, or the like can beused. The shape and constituent of the vaso-occlusive coil 30 willdepend upon the use to which the coil will be placed. For occludingperipheral or neural sites, the diameter of the wire used in theproduction of the coil 30 is preferably in the range of 0.001 to 0.006inches, and the outer diameter of the vaso-occlusive coil 30, itself, ispreferably in the range of 0.003 and 0.025 inches. For mostneurovascular applications, an outer diameter between 0.008 and 0.018inches provides sufficient hoop strength to hold the vaso-occlusive coil30 in place within the selected body site, without substantiallydistending the wall of the site and without moving from that site as aresult of the repetitive fluid pulsing found in the vascular system. Theaxial length of the wire used to make the vaso-occlusive coil 30 willusually fall in the range of 0.5 and 100 cm, more typically within therange of 2.0 and 40 cm. The axial length of the vaso-occlusive coil 30will usually fall within the range of 2 mm and 40 cm. It should be notedthat all of the dimensions provided for the vaso-occlusive coil 30 areprovided only as guidelines, and the invention, in its broadest aspects,should not be limited thereto. Rather, only dimensions that are suitablefor use in occluding sites within the human body are included in thescope of the invention. It should be appreciated that while the lengthof the vaso-occlusive coil 30 is shown in FIG. 1 as being on the sameorder of length as the pivotable coupling 26, the length of thevaso-occlusive coil 30 will typically be many orders greater than thatof the pivotable coupling 26.

Depending on the desired therapeutic effect and the shape of the site tobe treated, the vaso-occlusive coil 30 may be treated or accessorized innumerous ways in order to enhance its therapeutic effect. For example,the vaso-occlusive coil 30 may be made to form various secondary shapes,often through the use of heat treatment, that may be better suited tofill a particular treatment site, as disclosed in U.S. Pat. Nos.5,853,418 and 6,280,457, which are expressly incorporated herein byreference. Alternatively, the vaso-occlusive coil 30 may have little orno shape after introduction into the vascular space, as disclosed inU.S. Pat. No. 5,690,666, which is expressly incorporated herein byreference. In addition, external materials may be added to the outsideof vaso-occlusive coil 30 in an effort to increase its thrombolyticproperties. For example, fibrous materials can be tied or braided ontothe outside of the vaso-occlusive coil 30. These alternative embodimentsare disclosed in U.S. Pat. Nos. 5,226,911, 5,304,194, 5,354,295,5,382,259, 5,549,624, and 6,280,457, which are expressly incorporatedherein by reference.

Referring still to FIG. 1, the stretch-resisting member 34 is affixedbetween the distal end of the vaso-occlusive coil 30 and the distal endof the pivotable coupling 36 within the lumen 22 of the vaso-occlusivecoil 30 in a tensile relationship to prevent axial stretching of thevaso-occlusive coil 30. In the illustrated embodiment, thestretch-resisting member 34 comprises a distal cap 42 affixed outside ofthe distal end of the vaso-occlusive coil 30, and a looped thread 44coupled to the pivotable coupling 36 in a tensile relationship, suchthat the distal cap 42 is proximally urged against the distal end of thevaso-occlusive coil 30. The distal cap 42, which has a diameter greaterthan the diameter of the coil lumen 22, can be formed by gluing ormelting the distal end of the stretch-resisting member 34.Alternatively, the stretch-resisting member 34 may be tied in a knot(not shown), which may or may not be attached to the vaso-occlusive coil30.

In the illustrated embodiment, the stretch-resisting member 34 isfibrous and desirably polymeric. Suitable polymeric materials can beeither thermosetting or thermoplastic and can comprise a bundle ofthreads or a single filament. Themoplastics are preferred, because theyallow simplification of the procedure for constructing thestretch-resisting member, e.g., by allowing the distal cap 42 to beformed by melting using a simple tool, such as a soldering iron.Suitable polymers include most biocompatible materials that may be madein fibers, including thermoplastics, e.g., polyesters, such aspolyethyleneterephthalate (PET), especially Dacron®; polyamides,including Nylon®; polyolefins, such as polyethylene, polyprophylene,polybutylene, their mixtures, alloys, block, and random copolymers;fluoropolymers (polytetrafluoroethylene (PTFE)), or even silk orcollagen. The stretch-resisting member 34 may be composed frommaterials, such as dissolvable sutures, for instance, polylactic acid orpolyglycolic acid, to encourage cell growth in an aneurysm afterintroduction. Highly preferred is polypropylene, for instance, in theform of 10-0 and 9-0 polypropylene suture material. The diameter of thelooped thread 44 is typically between about 0.0001 inches and 0.01inches.

Alternatively, rather than using plastics, a wide variety of stainlesssteels can be used if some sacrifice in flexibility can be tolerated.Stretch-resisting members of this type are described in U.S. Pat. No.5,853,418, which is expressly incorporated herein by reference. Verydesirable materials of construction, from a mechanical point of view,are materials that maintain their shape despite being subject to highstress. Certain “super-elastic alloys” include various nickel-titaniumalloys (48-58 atomic % nickel and optionally containing modest amountsof iron); copper/zinc alloys containing 1-10 weight % of beryllium,silicon, tin, aluminum, or gallium; or nickel/aluminum alloys (36-38atomic % aluminum).

The pivotable coupling 36 comprises a proximal mounting coil 46 formedof a series of windings 50, a distal mounting coil 48 formed of a seriesof windings 52, and a flexible sleeve 54 for coupling the mounting coils46, 48 together. The proximal mounting coil 46 is mounted around thedistal end of the core wire 18 just distal to the severable junction 24,and the distal mounting coil 48 is mounted within the lumen 22 of thevaso-occlusive coil 30. The distal-most winding 52 of the distalmounting coil 48 is formed into a loop or hook 56, which is suitablyconnected to the looped thread 44 of the stretch-resisting member 34,thereby maintaining the stretch-resisting member 34 in a tensile state.

The mounting coils 46, 48 can be composed of the same material as thevaso-occlusive coil 30, but in the illustrated embodiment, are composedof platinum or platinum alloy. In the illustrated embodiment, thediameter of the wire used to make the mounting coils 46, 48 is smallerthan the diameters of the wire used to make the vaso-occlusive coil 30in order to minimize the profile of the pivotable coupling 36. The outerdiameter of the distal mounting coil 48 is preferably about the samesize as the diameter of the primary coil lumen 22, so that the distalmounting coil 48 and vaso-occlusive coil 30 snugly fit together.

The pivotable coupling 36 further comprises a core wire extension 58around which the distal mounting coil 48 is mounted to provide thedistal end of the pivotable coupling 36 the compressive strengthnecessary to prevent buckling when mounted within the lumen 22 of thevaso-occlusive coil 30. The mounting coils 46, 48 can be affixed to thecore wire 18, core wire extension 58, and vaso-occlusive coil 30 usingsuitable means, such as interference fitting, welding, or bonding.

The sleeve 54 is suitably mounted around the mounting coils 46, 48, andis composed of a highly flexible, yet axially strong material, such thatit is configured to axially connect the mounting coils 46, 48, whileallowing the mounting coils 46, 48 to pivot relative to each other aboutthe pivot point 38, as illustrated in FIG. 2. Suitable materials for thesleeve 54 include elastomeric polymers, which can be heat shrunk orotherwise bonded over the mounting coils 46, 48. Fibrous material mayalso be embedded within the sleeve 54 to increase its axial strength.The pivot point 38 can either be coincident within a space between theends of the mounting coils 46, 48 or a highly flexible material, such asan elastomeric polymer, that can be bonded between the mounting coils46, 48. As previously discussed, the outer diameters of the respectivemounting coils 46, 48 are preferably the same, so that the sleeve 54fits over the mounting coils 46, 48 in a uniformly snug manner.

Besides integrating the mounting coils 46, 48 in an axially fixed, butpivotably, relationship, the sleeve 54 also serves to electricallyinsulate the mounting coils 46, 48, as well as the distal end of thecore wire 18 and the core wire extension 58, from the bodily fluids inwhich they would otherwise be in contact with, so that the electrolyticprocess is focused at the severable junction 24. In addition, theproximal-most windings 40 of the vaso-occlusive coil 30 in which thedistal mounting coil 48 is affixed can be coated with an electricallyinsulative material, such as polyurethane or the like, to preventpotential electrical contact between the vaso-occlusive coil 30 and thecore wire 18.

Optional electrically conductive coils (not shown) can be mounted to thecoil wire 18 between the pivotable coupling 36 and the severablejunction 24 to provide a means to determine when the vaso-occlusivedevice 14 has detached from the core wire 18. That is, the electricallyconductive coils provide an increased conductance between the core wire18 and an external electrode, the substantial reduction of which can bemeasured when the conductive coils are eliminated from the electricalcircuit after the conductive coils (along with the vaso-occlusive device14) separates from the core wire 18.

Referring now to FIG. 3, a vaso-occlusive assembly 110 constructed inaccordance with another preferred embodiment is illustrated. Thevaso-occlusive assembly 110 is similar to the previously describedvaso-occlusive assembly 10, with the exception that it comprises avaso-occlusive device 114 that includes a different pivotable coupling36 for affixing the vaso-occlusive coil 30 to the core wire 18. Like thepreviously described pivotable coupling 36, the pivotable coupling 136illustrated in FIG. 3 has a proximal mounting coil 146 with windings 150affixed to the distal end of the core wire 18 and a distal mounting coil148 with windings 152 affixed within the lumen 22 of the vaso-occlusivecoil 30. These mounting coils 146, 148, however, are not connectedtogether via a sleeve-based pivotable coupling, but rather a link-basedpivotable coupling 136.

In particular, the pivotable coupling 136 comprises a loop member 154disposed through the lumen of the distal mounting coil 148, so thatproximal and distal eyelets 156, 158 respectively extend from theopposite sides of the distal mounting coil 148. The loop member 154 maybe suitably affixed within the lumen of the distal mounting coil 148using an interference fit or by bonding or welding. The pivotablecoupling 136 also comprises a hook 160 formed from the distal-mostwinding 150 of the proximal mounting coil 146. The hook 160 is linkedaround the proximal eyelet 156 of the loop member 154 to axially connectthe mounting coils 146, 148 to each other, while allowing the mountingcoils 146, 148 to pivot relative to each other about a pivot point 138,as illustrated in FIG. 4. Significantly, the hook 160 and proximaleyelet 156 are not welded or bonded together, so as to not hinder thepivoting action of the coupling 136.

Like the previously described pivotable coupling 36, the pivotablecoupling 136 in this case also serves as an anchoring assembly foranchoring the stretch-resisting member 34 within the vaso-occlusive coil30. In particular, the distal eyelet 158 of the looped member 154connects to the looped thread 44 of the stretch-resisting member 34 tomaintain the stretch-resisting member 34 in a tensile state. Themounting coil 146, the proximal loop 156 of the looped member 154, andthe proximal-most windings 40 of the vaso-occlusive coil 30 can becoated with an electrically insulative material (not shown), such aspolyurethane or the like, to prevent potential electrical contactbetween the vaso-occlusive coil 30 and the core wire 18. Optionally, themounting coil 146 can be left bare to provide a means to determine whenthe vaso-occlusive device 114 has detached from the core wire 18.

Referring now to FIG. 5, a vaso-occlusive assembly 210 constructed inaccordance with still another preferred embodiment is illustrated. Thevaso-occlusive assembly 210 is similar to the previously describedvaso-occlusive assemblies 10, 110, with the exception that it comprisesa vaso-occlusive device 214 with a different pivotable coupling 236 foraffixing a modified vaso-occlusive coil 230 to the core wire 18. Inparticular, the pivotable coupling 236 comprises a mounting coil 246having windings 250 affixed to proximal-most windings 240 of thevaso-occlusive coil 230 (mounting coil 246 and vaso-occlusive coil 230shown separately in FIG. 7), a pair of ball elements 256, 260 disposedon the respective distal end of the core wire 18 and proximal-mostwinding 250 of the mounting coil 246, and a flexible sleeve 254 forcoupling the ball elements 256, 260 together.

The mounting coil 246 and vaso-occlusive coil 230 are designed to beaffixed to each other in an interlocking manner. In particular, thewindings 246 of the mounting coil 230 and the proximal-most windings 240of the vaso-occlusive coil 230 are open-pitched (best shown in FIG. 7),so that the mounting coil windings 246 can be disposed within spaces 242between the open vaso-occlusive coil windings 240, and thevaso-occlusive coil windings 230 can likewise be disposed within spaces252 between the open mounting coil windings 250. It can be appreciated,that the mounting coil 246 and vaso-occlusive coil 230 can beinterlocked together using a twisting action, as illustrated in FIG. 7.To ensure that the mounting coil 246 and vaso-occlusive coil 230 remaininterlocked, they may be suitably welded or bonded together. Thecomposition and dimensions of the vaso-occlusive coil 230 may be similarto those of the previously described vaso-occlusive coil 30.

The mounting coil 246 preferably has a sufficient strength and stiffnessthat allows it to be integrated with the vaso-occlusive coil 230 in arobust manner. To this end, the windings 250 of the mounting coil 246are doubled up, so that the spaces 252 only exist between pairs ofwindings 250. That is, there are twice as many windings 250 as spaces252, thereby effectively increasing the strength of the mounting coil246 relative to the vaso-occlusive coil 230. To provide additionalstrength, the wire used to make the mounting coil 246 has an increaseddiameter relative to the diameter of the wire used to make thevaso-occlusive coil 230.

The outer diameters of the respective vaso-occlusive coil 230 andmounting coil 246 are selected to be the same, so that the outer profileof the combined assembly is uniform. The dimensions of the spaces 242between the open windings 240 of the vaso-occlusive coil 230 will dependon the size and number of windings 250 of the mounting coil 246, and thedimensions of the spaces 252 between the windings 250 of the mountingcoil 246 will likewise depend on the size and number of windings 240 ofthe vaso-occlusive coil 230. In the illustrated embodiment, the width ofthe spaces 242, 252 of one coil 230, 246 will be selected toconveniently accommodate the windings 250, 240 of the other coil 246,230, so that a substantial axial force is not exerted on the respectivewindings of the coils 230, 246. Thus, the width of the spaces 242between the windings 240 of the vaso-occlusive coil 230 will be aboutequal to twice the diameter of the wire used to make the mounting coil246, whereas the width of the spaces 252 between the windings 250 of themounting coil 246 will be about equal to the diameter of the wire usedto make the vaso-occlusive coil 230.

The ball members 256, 260 may be formed, e.g., by melting the ends ofthe respective core wire 18 and mounting coil 246. The sleeve 254 issuitably mounted around the ball members 254, 260, and is composed of ahighly flexible, yet axially strong material, such that it is configuredto axially connect the ball members 254, 260 while allowing the ballmembers 254, 260 to pivot relative to each other about a pivot point238, as illustrated in FIG. 6.

The pivotable coupling 236, like the pivotable couplings 36,136described above, additionally serves as an anchoring assembly thatanchors the stretch-resisting member 34 within the vaso-occlusive coil230. To this end, the doubling of the mounting coil windings 250naturally forms an eyelet 255 (best shown in FIG. 7) at the distal endof the mounting coil 246 that is suitably connected to the looped thread44 of the stretch-resisting member 34, thereby maintaining thestretch-resisting member 34 in a tensile state.

In the illustrated embodiment, the sleeve 254 comprises a mesh materialto provide the sleeve 254 with maximum flexibility. Because, the meshsleeve 254 does not electrically isolate the ball members 256, 260, theball members 256, 260 can be coated with an electrically insulativematerial (not shown), such as polyurethane or the like, to preventpotential electrical contact between the vaso-occlusive coil 230 and thecore wire 18. Optionally, the proximal ball member 256 can be left bareto provide a means to determine when the vaso-occlusive device 214 hasdetached from the core wire 18.

Referring now to FIG. 8, a vaso-occlusive assembly 310 constructed inaccordance with yet another preferred embodiment is illustrated. Thevaso-occlusive assembly 310 is similar to the previously describedvaso-occlusive assemblies 10, 110, 210, with the exception that itcomprises a vaso-occlusive device 314 with a different pivotablecoupling 336 for affixing a modified vaso-occlusive coil 330 to the corewire 18. In particular, the pivotable coupling 336 comprises a proximalmounting coil 346 with windings 350 affixed to the distal end of thecore wire 18, and a distal mounting coil 338 within windings 352 affixedto the windings 350 of the proximal mounting coil 346 and windings 340of the vaso-occlusive coil 330 (mounting coils 346, 348 andvaso-occlusive coil 330 shown separately in FIG. 10).

Like the previously described mounting coil 246 and vaso-occlusive coil230, the mounting coils 346, 348 and vaso-occlusive coil 330 aredesigned to be affixed to each other in an interlocking manner. Inparticular, the distal-most windings 350 of the proximal mounting coil346, all of the windings 350 of the distal mounting coil 346, and theproximal-most windings 340 of the vaso-occlusive coil 330 areopen-pitched (best shown in FIG. 10). In this manner, the distal-mostcoil windings 350 of the proximal mounting coil 346 can be disposedwithin spaces 356 between the proximal-most windings 352 of the distalmounting coil 348, and the proximal-most windings 352 of the distalmounting coil 348 can likewise be disposed within spaces 354 between thedistal-most coil windings 350 of the proximal mounting coil 346. In asimilar manner, the proximal-most windings 340 of the vaso-occlusivecoil 330 can be disposed within the spaces 356 between the distal-mostwindings 352 of the distal mounting coil 348, and the distal-mostwindings 352 of the distal mounting coil 348 can likewise be disposedwithin spaces 342 between the proximal-most windings 340 of thevaso-occlusive coil 330.

It can be appreciated, that the distal and proximal mounting coils 346,348 and vaso-occlusive coil 330 can be interlocked together using atwisting action, as illustrated in FIG. 10. To ensure that the distaland proximal mounting coils 346, 348 and vaso-occlusive coil 330 remaininterlocked, they may be suitably welded or bonded together. Thecomposition and dimensions of the vaso-occlusive coil 330 may be similarto those of the previously described vaso-occlusive coil 30.

The outer diameters of the distal and proximal mounting coils 346, 348and vaso-occlusive coil 330 are selected to be the same, so that theouter profile of the combined assembly is uniform. In the same mannerdescribed above with respect to the mounting coil 246 and vaso-occlusivecoil 230, the dimensions of the spaces between the open windings of eachcoil will depend on the size and number of the windings of the coil thatinterlocks with the respective coil.

The number of windings of the distal mounting coil 348 is greater thanthe combined number of windings of the proximal mounting coil 346 andvaso-occlusive coil 330, so that the spaces between the windings at thecenter of the distal mounting coil 346 remain empty. In this manner, apivot point 338 about which the proximal and distal portions of thedistal mounting coil 348 may pivot, is formed in the center of thedistal mounting coil 348.

The pivotable coupling 336, like the pivotable couplings 36, 136, 236described above, additionally serves as an anchoring assembly thatanchors the stretch-resisting member 34 within the vaso-occlusive coil330. To this end, the proximal mounting coil 346 is formed by coilingthe distal end of the core wire 18 onto itself, as illustrated in FIG.10. An eyelet 358 is formed at the distal end of the proximal mountingcoil 348 where the core wire 18 coils back is suitably connected to thelooped thread 44 of the stretch-resisting member 34, thereby maintainingthe stretch-resisting member 34 in a tensile state.

The proximal and distal mounting coils 346, 348 and the proximal-mostwindings 340 of the vaso-occlusive coil 330 can be coated with anelectrically insulative material (not shown), such as polyurethane orthe like, to prevent potential electrical contact between thevaso-occlusive coil 330 and the core wire 18. The distal portion of thecore wire 18 extending through the proximal mounting coil 346 may alsobe coated with an electrically insulative material. Optionally, thisportion of the core wire 18 can be left bare to provide a means todetermine when the vaso-occlusive device 314 has detached from the corewire 18.

Although the pivotable couplings of the previous vaso-occlusiveassemblies have been described as being located distal to the severablejunction, pivotable couplings can also be located proximal to theseverable junction.

Having described the structure of the vaso-occlusive assemblies, theoperation of the vaso-occlusive assembly 100 in occluding a vascularsite, and in particular, an aneurysm 400 originating from a parent bloodvessel 402, will now be described with reference to FIGS. 11A-11C. Thevaso-occlusive assemblies 110, 210, 310 can similarly be used to occludethe aneurysm 400, but for purposes of brevity, only the use of thevaso-occlusive assembly 10 will be described.

First, in a conventional manner, the catheter 16, which houses the corewire 18 and vaso-occlusive coil 14, is introduced through thevasculature of the patient and manipulated until the distal end of thecatheter 16 resides within a neck 402 of the aneurysm 400 (FIG. 11A). Atthis point, the vaso-occlusive coil 14 is positioned at the distal endof the catheter 16 in its undeployed state. The core wire 18 is thenpushed in the distal direction, causing the vaso-occlusive coil 14 toextend out of the distal end of the catheter 16 and deploy within a sacof the 404 of the aneurysm 400 (FIG. 11B). A current is then applied tothe core wire 18 (via the electrode 26 illustrated in FIG. 1), whichcauses the severable junction 24 to disintegrate via electrolysis, afterwhich the vaso-occlusive coil 14 detaches from the core wire 18 (FIG.11C). During detachment, the vaso-occlusive coil 14 creates an axialforce in the proximal direction that causes the flexible coupling 36 tobuckle, thereby deflecting the axial force in the lateral direction, sothat the catheter 16 is not displaced from the aneurysmal neck 404 bythe axial force.

Additional vaso-occlusive coils 14 can be deployed within the aneurysmalsac 402 in a similar manner to completely occlude the aneurysm 400.After occlusion of the aneurysm 400 is completed, the vaso-occlusionassembly 10 is removed from the vasculature of the patient.

Although particular embodiments of the present invention have been shownand described, it will be understood that it is not intended to limitthe present invention to the preferred embodiments, and it will beobvious to those skilled in the art that various changes andmodifications may be made without departing from the spirit and scope ofthe present invention. Thus, the present inventions are intended tocover alternatives, modifications, and equivalents, which may beincluded within the spirit and scope of the present invention as definedby the claims.

1. An assembly for occluding a vascular site of a human or veterinarypatient, the assembly comprising: a vaso-occlusive member; a pushermember having a distal end and a severable junction located proximal tothe distal end; and a pivotable coupling that couples the pusher memberto the occlusive member, wherein the pivotable coupling comprises aproximal link member coupled to the pusher member distal end, and adistal link member coupled to the vaso-occlusive member, wherein therespective proximal and distal link members pivotably engage each other.2. The assembly of claim 1, wherein the proximal and distal link membersare hooks or loops.
 3. The assembly of claim 1, further comprising aproximal coil coupled to the pusher member distal end, wherein theproximal link member is disposed on a distal end of the proximal coil;and a distal coil coupled to the vaso-occlusive member, wherein thedistal link member is disposed on a proximal end of the distal coil. 4.The assembly of claim 1, wherein the severable junction comprises amechanically severable junction.
 5. The assembly of claim 1, wherein theseverable junction comprises an electrolytically severable junction. 6.The assembly of claim 1, wherein the vaso-occlusive member comprises acoil.
 7. The assembly of claim 4, further comprising a stretch-resistingmember, wherein the pivotable coupling anchors the stretch-resistingmember within a lumen of the coil.
 8. The assembly of claim 1, whereinthe pivotable coupling comprises an element that electrically insulatesthe pusher member distal end from vaso-occlusive member.
 9. The assemblyof claim 1, further comprising a catheter having a delivery lumen inwhich the pusher member is slidably disposed.
 10. A method of occludinga vascular site using the assembly of claim 1, the method comprising:manipulating the pusher member to place the vaso-occlusive memberadjacent the vascular site; severing the severable junction to detachthe vaso-occlusive member from the pusher member, wherein an axial forceis applied by the vaso-occlusive member in a proximal direction; andbuckling the pivotable coupling to laterally deflect the axial force.11. A method of occluding a vascular site using the assembly of claim 9,wherein the vascular site comprises an aneurysm having an aneurysmal sacand an aneurysmal neck, the method comprising: locating the catheterwithin the aneurysmal neck; manipulating the pusher member to place thevaso-occlusive member within the aneurysmal sac; severing the severablejunction to detach the vaso-occlusive member from the pusher member,wherein an axial force is applied by the vaso-occlusive member in aproximal direction; and buckling the pivotable coupling to laterallydeflect the axial force, wherein the catheter is not displaced from theaneurysmal neck by the axial force.